Wolframin mutations and hospitalization for psychiatric illness (original) (raw)
Inoue H, Tanizawa Y, Wasson J, Behn P, Kalidas K, Bernal-Mizrachi E et al. A gene encoding a transmembrane protein is mutated in patients with diabetes mellitus and optic atrophy (Wolfram syndrome). Nat Genet 1998; 20: 143–148. ArticleCAS Google Scholar
Strom TM, Hortnagel K, Hofmann S, Gekeler F, Scharfe C, Rabl W et al. Diabetes insipidus, diabetes mellitus, optic atrophy and deafness (DIDMOAD) caused by mutations in a novel gene (wolframin) coding for a predicted transmembrane protein. Hum Mol Genet 1998; 7: 2021–2028. ArticleCAS Google Scholar
Swift RG, Sadler DB, Swift M . Psychiatric findings in Wolfram syndrome homozygotes. Lancet 1990; 336: 667–669. ArticleCAS Google Scholar
Swift RG, Perkins DO, Chase CL, Sadler DB, Swift M . Psychiatric disorders in 36 Wolfram syndrome families. Am J Psychiatry 1991; 148: 775–779. ArticleCAS Google Scholar
Swift RG, Polymeropoulos M, Torres R, Swift M . Predisposition of Wolfram syndrome heterozygotes to psychiatric illness. Mol Psychiatry 1998; 3: 86–91. ArticleCAS Google Scholar
Swift M, Swift RG . Psychiatric disorders and mutations at the Wolfram syndrome locus. Biol Psychiatry 2000; 47: 787–793. ArticleCAS Google Scholar
Takeda K, Inoue H, Tanizawa Y, Matsuzaki Y, Oba J, Watanabe Y et al. WFS1 (Wolfram syndrome 1) gene product: predominant subcellular localization to endoplasmic reticulum in cultured cells and neuronal expression in rat brain. Hum Mol Genet 2001; 10: 477–484. ArticleCAS Google Scholar
Wolfram DJ . Diabetes mellitus and simple optic atrophy among siblings: report of four cases. Staff Proc Mayo Clin 1938; 13: 715–718. Google Scholar
Cremers CWRJ, Wijdeveld PGAB, Pinckers AJLG . Juvenile diabetes mellitus, optic atrophy, hearing loss, diabetes insipidus, atonia of the urinary tract and bladder, and other abnormalities (Wolfram Syndrome). Acta Paed Scand 1977; 264 (Suppl): 3–16. Google Scholar
Kinsley BT, Swift M, Dumont RH, Swift RG . Morbidity and mortality in the Wolfram syndrome. Diabetes Care 1995; 18: 1566–1570. ArticleCAS Google Scholar
van ven Ouweland JM, Cryns K, Pennings RJ, Walraven I, Janssen GM, Maassen JA et al. Molecular characterization of WFS1 in patients with Wolfram syndrome. J Mol Diagn 2003; 5: 88–95. Article Google Scholar
Torres R, Leroy E, Hu X, Katrivanou A, Gourzis P, Papachatzopoulou A et al. Mutation screening of the Wolfram syndrome gene in psychiatric patients. Mol Psychiatry 2001; 6: 39–43. ArticleCAS Google Scholar
Crawford J, Zielinski MA, Fisher LJ, Sutherland GR, Goldney RD . Is there a relationship between Wolfram syndrome carrier status and suicide? Am J Med Genet 2002; 114: 343–346. Article Google Scholar
Furlong RA, Ho LW, Rubinsztein JS, Michael A, Walsh C, Paykel ES et al. A rare coding variant within the wolframin gene in bipolar and unipolar affective disorder cases. Neurosci Lett 1999; 277: 123–126. ArticleCAS Google Scholar
Serretti A, Cusin C, Cristina S, Lorenzi C, Lilli R, Lattuada E et al. Multicentre Italian family-based association study on tyrosine hydroxylase, catechol-_O_-methyl transferase and Wolfram syndrome 1 polymorphisms in mood disorders. Psychiatr Genet 2003; 13: 121–126. PubMed Google Scholar
Kato T, Iwamoto K, Washizuka S, Mori K, Tajima O, Akiyama T et al. No association of mutations and mRNA expression of WFS1/wolframin with bipolar disorder in humans. Neurosci Lett 2003; 338: 21–24. ArticleCAS Google Scholar
Sequeira A, Kim C, Seguin M, Lesage A, Chawky N, Desautels A et al. Wolfram syndrome and suicide: evidence for a role of WFS1 in suicidal and impulsive behavior. Am J Med Genet 2003; 119B: 108–113. Article Google Scholar
Deng H-W . Population admixture may appear to mask, change or reverse genetic effects of genes underlying complex traits. Genetics 2001; 159: 1319–1323. CASPubMedPubMed Central Google Scholar
Emahazion T, Feuk L, Jobs M, Sawyer SL, Fredman D, St Clair D et al. SNP association studies in Alzheimer's disease highlight problems for complex disease analysis. Trends Genet 2001; 17: 407–413. ArticleCAS Google Scholar
Marchini J, Cardon LR, Phillips MS, Donnelly P . The effects of human population structure on large genetic association studies. Nat Genet 2004; 36: 512–517. ArticleCAS Google Scholar
Middle F, Jones I, McCandless F, Barrett T, Khanim F, Owen MJ . Bipolar disorder and variation at a common polymorphism (A1832G) within exon 8 of the Wolfram gene. Am J Med Genet 2000; 96: 154–157. ArticleCAS Google Scholar
Martorell L, Zaera MG, Valero J, Serrano D, Figuera L, Joven J . The WFS1 (Wolfram syndrome 1) is not a major susceptibility gene for the development of psychiatric disorders. Psychiatr Genet 2003; 13: 29–32. Article Google Scholar
Ohtsuki T, Ishiguro H, Yoshikawa T, Arinami T . WFS1 gene mutation search in depressive patients: detection of five missense polymorphisms but no association with depression or bipolar affective disorder. J Affect Disord 2000; 58: 11–17. ArticleCAS Google Scholar
Evans KL, Lawson D, Meitinger T, Blackwood DH, Porteous DJ . Mutational analysis of the Wolfram syndrome gene in two families with chromosome 4p-linked bipolar affective disorder. Am J Med Genet 2000; 96: 158–160. ArticleCAS Google Scholar
Athma P, Rappaport R, Swift M . Molecular genotyping shows that ataxia-telangiectasia heterozygotes are predisposed to breast cancer. Cancer Genet Cytogenet 1996; 92: 130–134. ArticleCAS Google Scholar
Dork T, Bendix R, Bremer M, Rades D, Klopper K, Nicke M et al. Spectrum of ATM gene mutations in a hospital-based series of unselected breast cancer patients. Cancer Res 2001; 61: 7608–7615. CAS Google Scholar
Li A, Swift M . Mutations at the ataxia-telangiectasia locus and clinical phenotypes of A-T patients. Am J Med Genet 2000; 92: 170–177. ArticleCAS Google Scholar
Dork T, Bendix-Waltes R, Wegner RD, Stumm M . Slow progression of ataxia-telangiectasia with double missense and in frame splice mutations. Am J Med Genet 2004; 126A: 272–277. Article Google Scholar